Abstract
The localization of mRNA expression in the mammary gland is technically challenging due to the unique structural problems posed by breast tissues. These include closely interdigitated and sparse layers of tissue, high levels of extracellular matrix, and large quantities of adipose tissue. This chapter describes an in situ hybridization method using radiolabeled oligonucleotides that was developed to allow the detection of the rarest of messenger RNAs in many types of breast sample.
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Abbreviations
- (BCIP/NBT):
-
bromochloroindolyl phosphate/nitro blue tetrazolium
- (DEPC):
-
diethyl pyrocarbonate
- (DIG):
-
digoxigenin
- (EST):
-
expressed sequence tag
- (ISH):
-
in situ hybridization
- (PFA):
-
paraformaldehyde
- (PBS):
-
phosphate buffered saline
- (TGF):
-
transforming growth factor
- (SSC):
-
0.15 M sodium chloride/sodium citrate pH 7.0
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Weber-Hall, S., Dale, T. (2000). mRNA In Situ Hybridization in the Mammary Gland. In: Ip, M.M., Asch, B.B. (eds) Methods in Mammary Gland Biology and Breast Cancer Research. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-4295-7_19
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DOI: https://doi.org/10.1007/978-1-4615-4295-7_19
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4613-6927-1
Online ISBN: 978-1-4615-4295-7
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